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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
Jason Homsy, Samir Zaidi, Yufeng Shen, et al.
Science (2015) Vol. 350, Iss. 6265, pp. 1262-1266
Open Access | Times Cited: 763

Showing 1-25 of 763 citing articles:

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
Sheng Chih Jin, Jason Homsy, Samir Zaidi, et al.
Nature Genetics (2017) Vol. 49, Iss. 11, pp. 1593-1601
Open Access | Times Cited: 765
Evaluation and Management of the Child and Adult With Fontan Circulation: A Scientific Statement From the American Heart Association
Jack Rychik, Andrew M. Atz, David S. Celermajer, et al.
Circulation (2019) Vol. 140, Iss. 6
Open Access | Times Cited: 706
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association
Mary Ella Pierpont, Martina Brueckner, Wendy K. Chung, et al.
Circulation (2018) Vol. 138, Iss. 21
Open Access | Times Cited: 532
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Holly A.F. Stessman, Bo Xiong, Bradley P. Coe, et al.
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 515-526
Open Access | Times Cited: 512
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
Slavé Petrovski, Vimla S. Aggarwal, Jessica L. Giordano, et al.
The Lancet (2019) Vol. 393, Iss. 10173, pp. 758-767
Closed Access | Times Cited: 499
Genetics and Genomics of Congenital Heart Disease
Samir Zaidi, Martina Brueckner
Circulation Research (2017) Vol. 120, Iss. 6, pp. 923-940
Open Access | Times Cited: 481
New insights into the generation and role of de novo mutations in health and disease
Rocío Acuña‐Hidalgo, Joris A. Veltman, Alexander Hoischen
Genome biology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 422
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
Alejandro Sifrim, Marc‐Phillip Hitz, Anna Wilsdon, et al.
Nature Genetics (2016) Vol. 48, Iss. 9, pp. 1060-1065
Open Access | Times Cited: 420
Single-Cell Resolution of Temporal Gene Expression during Heart Development
Daniel M. DeLaughter, Alexander G. Bick, Hiroko Wakimoto, et al.
Developmental Cell (2016) Vol. 39, Iss. 4, pp. 480-490
Open Access | Times Cited: 410
SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research
Pamela Feliciano, Amy M. Daniels, LeeAnne Green Snyder, et al.
Neuron (2018) Vol. 97, Iss. 3, pp. 488-493
Open Access | Times Cited: 399
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A. Kosmicki, Kaitlin E. Samocha, Daniel P. Howrigan, et al.
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 504-510
Open Access | Times Cited: 342
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
EP Europace (2022) Vol. 24, Iss. 8, pp. 1307-1367
Open Access | Times Cited: 259
Trends in Congenital Heart Disease
John K. Triedman, Jane W. Newburger
Circulation (2016) Vol. 133, Iss. 25, pp. 2716-2733
Open Access | Times Cited: 243
A map of constrained coding regions in the human genome
James M. Havrilla, Brent S. Pedersen, Ryan M. Layer, et al.
Nature Genetics (2018) Vol. 51, Iss. 1, pp. 88-95
Open Access | Times Cited: 236
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders
Víctor Faúndes, William G. Newman, Laura Bernardini, et al.
The American Journal of Human Genetics (2017) Vol. 102, Iss. 1, pp. 175-187
Open Access | Times Cited: 235
denovo-db: a compendium of humande novovariants
Tychele N. Turner, Yi Qian, Niklas Krumm, et al.
Nucleic Acids Research (2016) Vol. 45, Iss. D1, pp. D804-D811
Open Access | Times Cited: 192
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles
Andrew T. Timberlake, Jungmin Choi, Samir Zaidi, et al.
eLife (2016) Vol. 5
Open Access | Times Cited: 185
Rare-variant collapsing analyses for complex traits: guidelines and applications
Gundula Povysil, Slavé Petrovski, Joseph Hostyk, et al.
Nature Reviews Genetics (2019) Vol. 20, Iss. 12, pp. 747-759
Closed Access | Times Cited: 183
Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Deidre R. Krupp, Rebecca Barnard, Yannis Duffourd, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 3, pp. 369-390
Open Access | Times Cited: 179
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
A. Jeremy Willsey, Thomas Fernandez, Dongmei Yu, et al.
Neuron (2017) Vol. 94, Iss. 3, pp. 486-499.e9
Open Access | Times Cited: 173
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
Donna J. Page, Matthieu J. Miossec, Simon G. Williams, et al.
Circulation Research (2019) Vol. 124, Iss. 4, pp. 553-563
Open Access | Times Cited: 161
Genomic frontiers in congenital heart disease
Sarah U. Morton, Daniel Quiat, Jonathan G. Seidman, et al.
Nature Reviews Cardiology (2021) Vol. 19, Iss. 1, pp. 26-42
Open Access | Times Cited: 160
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Heart Rhythm (2022) Vol. 19, Iss. 7, pp. e1-e60
Open Access | Times Cited: 160
Does general anesthesia affect neurodevelopment in infants and children?
Mary Ellen McCann, Sulpicio G. Soriano
BMJ (2019), pp. l6459-l6459
Closed Access | Times Cited: 159
MVP predicts the pathogenicity of missense variants by deep learning
Hongjian Qi, Haicang Zhang, Yige Zhao, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 153
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